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Microbiology 153 (2007), 1350-1360; DOI  10.1099/mic.0.2006/003707-0
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Microbiology 153 (2007), 1350-1360; DOI  10.1099/mic.0.2006/003707-0
© 2007 Society for General Microbiology

Analysis of the expression, regulation and export of NleA–E in Escherichia coli O157 : H7

Andrew J. Roe1,{dagger}, Luke Tysall1,{dagger}, Tracy Dransfield1, Dai Wang1, Douglas Fraser-Pitt2, Arvind Mahajan1,2, Chrystala Constandinou3, Neil Inglis2, Alison Downing4, Richard Talbot4, David G. E. Smith2,5 and David L. Gally1

1 Zoonotic and Animal Pathogens Research Laboratory, Centre for Infectious Disease, The Chancellor's Building, 49 Little France Crescent, Edinburgh EH16 4SB, UK
2 Moredun Research Institute, Pentlands Science Park, Bush Loan, Penicuik, Midlothian EH26 0PZ, UK
3 School of Biosciences, University of Birmingham, Birmingham B15 2TT, UK
4 Roslin Institute, Roslin BioCentre, Midlothian EH25 9PS, UK
5 Institute for Comparative Medicine, University of Glasgow, Glasgow G61 1QH, UK

Correspondence
David L. Gally
d.gally{at}ed.ac.uk

Previous work has shown that locus of enterocyte effacement (LEE)-encoded effector proteins such as Tir and Map can be exported via the type III secretion system (T3SS) of Escherichia coli O157 : H7. Additionally, a family of non-LEE-encoded (Nle) effector proteins has been shown to be secreted from Citrobacter rodentium, homologues of which are located on the E. coli O157 chromosome. While NleA has been shown to be secreted from pathogenic E. coli, the secretion of other Nle effector proteins has only been detected under induced conditions, or using a mutated T3SS. This study aimed to determine: (1) which nle genes are expressed in E. coli O157 : H7 under secretion-permissive conditions; (2) if Nle proteins are secreted from wild-type E. coli O157 : H7 under secretion-permissive conditions; and (3) if nle gene expression is regulated co-ordinately with other LEE-encoded effectors. Using data generated from a combination of transcriptome arrays, reporter fusions and proteomics, it was demonstrated that only nleA is expressed co-ordinately with the LEE. Secretion and expression of NleA were regulated directly or indirectly by ler, a key activator of the LEE. MS confirmed the secretion of NleA into the culture supernatant, while NleB–F were not detected.


Abbreviations: eGFP, enhanced green fluorescent protein; EHEC, enterohaemorrhagic Escherichia coli; EPEC, enteropathogenic Escherichia coli; GFP, green fluorescent protein; LEE, locus of enterocyte effacement; RFP, red fluorescent protein; T3, type III; T3SS, type III secretion system

{dagger}These authors contributed equally to this work.

The array data discussed in this publication have been deposited in the NCBI Gene Expression Omnibus (GEO; http://www.ncbi.nlm.nih.gov/geo/) and are accessible through GEO series accession number GSE6296.




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J. Bacteriol.Home page
V. A. Garcia-Angulo, W. Deng, N. A. Thomas, B. B. Finlay, and J. L. Puente
Regulation of Expression and Secretion of NleH, a New Non-Locus of Enterocyte Effacement-Encoded Effector in Citrobacter rodentium
J. Bacteriol., April 1, 2008; 190(7): 2388 - 2399.
[Abstract] [Full Text] [PDF]




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